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Eine direkte, regioselektive und atomökonomische Synthesevon 3-Aroyl-N-Hydroxy-5-Nitroindolen durch Cycloaddition von 4-Nitronitrosobenzol mit Alkynonen

Article DOI: 10.3791/60201-v • 07:30 min • January 21st, 2020
January 21st, 2020 •
1, 1, 1, 1, 2, 1
1Dipartimento di Scienza e Alta Tecnologia, Università degli Studi dell'Insubria, 2Department of Chemistry and Biochemistry, University of Oklahoma, Stephenson Life Sciences Research Center

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3-Aroyl-N-Hydroxy-5-Nitroindole wurden durch Cycloaddition von 4-Nitronitrosobenzol mit einem konjugierten terminalen Alkyn in einem einstufigen thermischen Verfahren synthetisiert. Die Vorbereitung des Nitrosarens und der Alkynone wurde angemessen und jeweils durch Oxidationsverfahren an der entsprechenden Aniline und am Alkyno berichtet.

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Chemie Ausgabe 155 3-Aroylindole N-Hydroxyindole Nitrosoaren Alkynone Annulation Cycloaddition Alkynole Aniline
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